FDA UDI In Commercial Distribution 🇺🇸 United States

Eko Mobile App iOS

DI: 00863609000334 · Model: 3.1.1 · Eko Devices, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Eko Mobile App iOS
Primary DI
00863609000334
Version / Model
3.1.1
Company Name
Eko Devices, Inc.
Labeler DUNS
079670921
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-16
Public Version
3
Public Version Date
2021-04-12
Public Version Status
Update
Public Device Record Key
0dc24928-1f99-41c6-9674-8e12da00e124

Device Description

iOS mobile device software for use with Eko products.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OUG Medical Device Data System

GMDN Terms

Code Name
57967 Medical equipment clinical data interfacing software

Identifiers

Type ID
Primary 00863609000334